Clark Sarah, Schwalbe Jennifer, Stasko Melissa R, Yarowsky Paul J, Costa Alberto C S
Department of Pharmacology and Exp. Therapeutics, University of Maryland School of Medicine, Baltimore, MD 21201-1509, USA.
Exp Neurol. 2006 Jul;200(1):256-61. doi: 10.1016/j.expneurol.2006.02.005. Epub 2006 Apr 19.
The Ts65Dn mouse, an adult model of Down syndrome displays behavioral deficits consistent with a dysfunctional hippocampus, similar to that seen with DS. In looking for mechanisms underlying these performance deficits, we have assessed adult neurogenesis in the dentate gyrus of Ts65Dn. Under untreated conditions, Ts65Dn mice (2-5 months old) showed markedly fewer BrdU-labeled cells than euploid animals. Chronic antidepressant treatment for over 3 weeks with the serotonin selective reuptake inhibitor, fluoxetine, increased neurogenesis in the Ts65Dn to comparable levels seen in the euploid by augmenting both proliferation and survival of BrdU-labeled cells in the subgranular layer and granule cell layer of the hippocampus, respectively.
Ts65Dn小鼠是唐氏综合征的成年模型,表现出与海马体功能失调一致的行为缺陷,类似于唐氏综合征患者所见。在寻找这些行为缺陷背后的机制时,我们评估了Ts65Dn小鼠齿状回中的成年神经发生。在未经治疗的条件下,2至5个月大的Ts65Dn小鼠的BrdU标记细胞明显少于整倍体动物。用5-羟色胺选择性再摄取抑制剂氟西汀进行超过3周的慢性抗抑郁治疗,通过分别增加海马体颗粒下层和颗粒细胞层中BrdU标记细胞的增殖和存活,使Ts65Dn小鼠的神经发生增加到与整倍体动物相当的水平。